Variant report

Variant	rs568470527
Chromosome Location	chr1:63217035-63217036
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3333680	chr1:63216564-63218512	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv1616688	chr1:63217025-63217039	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63208800-63220400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:63211000-63222200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:63212400-63218600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:63216400-63217200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:63216600-63217200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:63216800-63217200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:63216800-63217200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:63216800-63217200	Enhancers	Adipose Nuclei	Adipose
9	chr1:63216800-63217200	Enhancers	HSMMtube	muscle
10	chr1:63217000-63217800	Enhancers	Liver	Liver
11	chr1:63217000-63217800	Enhancers	Ovary	ovary
12	chr1:63217000-63218400	Enhancers	Aorta	Aorta

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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